Styrenes
Indofine Chemical 3-Fluorostyrene, 98%, 5 Gm
3-FLUOROSTYRENE 5 GM, Fluoro Organics, 1-Fluoro-3-vinylbenzene, C8H7F, MW: 122.14, 0.98, 350-51-6, MFCD00000341
![Sigma Aldrich Fine Chemicals Biosciences (RP)-1-[(R)-alpha-(Dimethylamino)-2-(diphenylphosphino)benzyl]-2-diphenylphosphinoferrocene optical purity ee: >=99% | 1003012-96-1 | 100MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/501861629.PNG-250.jpg)
Sigma Aldrich Fine Chemicals Biosciences (RP)-1-[(R)-alpha-(Dimethylamino)-2-(diphenylphosphino)benzyl]-2-diphenylphosphinoferrocene optical purity ee: >=99% | 1003012-96-1 | 100MG
(RP)-1-[(R)-alpha-(Dimethylamino)-2-(diphenylphosphino)benzyl]-2-diphenylphosphinoferrocene optical purity ee: >=99% | Mol Wt: 687.57 | 1003012-96-1 | 100MG
eMolecules (-)-(R)-4-BROMOSTYRENE OXIDE IN HEXANE (1:1 W/W) | 62566-68-1 | MFCD08277298 | 1g
AstaTech | (-)-(R)-4-BROMOSTYRENE OXIDE IN HEXANE (1:1 W/W) | 1g | 112523457 | 54596 | 95.000 | 62566-68-1 | MFCD08277298 | 199.047 | C8H7BrO
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Pfaltz & Bauer 1 6-Diphenylhexatriene 98%| 1G | 1720-32-7
1 6-Diphenylhexatriene 98%| 1G | 1720-32-7
Apexbio Technology LLC NMS-873 1418013-75-8 10mM (in 1mL DMSO)
NMS-873 (CAS 1418013-75-8) is a selective inhibitor of the ATPase VCP/p97 demonstrating inhibitory activity with an IC50 value of 30 nM It targets wild-type VCP as well as VCPC522T mutants without disrupting VCP oligomerization NMS-873 exhibits selectivity against other AAA ATPases HSP90 and various kinases In tumor cell lines including HCT-116 treatment with NMS-873 induces accumulation of polyubiquitinated proteins and stabilization of cyclin E and Mcl-1 leading to altered cell-cycle distribution and reduced cell proliferation NMS-873 shows cytotoxicity across blood cancer and solid tumor cell models (IC50 values 0 08 2 M) supporting its utility in oncology research
Medchemexpress LLC PFI-653 (Vanin-1-IN-1) | 2173134-00-2 | 99.9% | 25 MG
PFI-653 is a chemical probe and a vanin-1 inhibitor. It binds to plasma vanin-1 from mouse, rat, dog, and human. Vanin-1 is a cell surface-associated inositol (GPi)-anchored protein crucial in metabolism and inflammation.
- Binds to plasma vanin-1 from multiple species
- Inhibits vanin-1, a GPi-anchored protein important in metabolism and inflammation
- Exhibits nanomolar IC50 values for vanin-1 inhibition across species
eMolecules AstaTech / 4-METHOXY-4-NITROSTILBENE / 0.25g / 721754762 / D91422 / 95.000 / 1472-68-0 / MFCD00143335 / 255.273 / C15H13NO3
AstaTech / 4-METHOXY-4-NITROSTILBENE / 0.25g / 721754762 / D91422 / 95.000 / 1472-68-0 / MFCD00143335 / 255.273 / C15H13NO3
TARGETMOL CHEMICALS INC PIPERAQUINE TETRAPHOSPHA 25MG
Also available in 5 mg 10 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Piperaquine tetraphosphate tetrahydrate is a potent anti-parasites agent. purity: 98%
Strem, An Ascensus Company CAS# 52522-40-4. Tris(dibenzylideneacetone)dipalladium(0) chloroform adduct. MFCD00075479. 10G
CAS# 52522-40-4. 10G. Tris(dibenzylideneacetone)dipalladium(0) chloroform adduct. MFCD00075479. Molecular Formula: C52H43Cl3O3Pd2. Molecular Weight: 1035.08. Color/Form: red to brown solid. Stability: air sensitive, moisture sensitive. Strem#: 46-3010 www.strem.com/catalog/v3/46-3010/
Apexbio Technology LLC CPI-637 1884712-47-3 10mg
CPI-637 (CAS 1884712-47-3) is a selective small molecule inhibitor targeting the bromodomains of CBP (CREB-binding protein) and EP300 with IC50 values of 0 03 M and 11 0 M respectively It demonstrates over 700-fold selectivity for CBP/EP300 bromodomains relative to the BET bromodomain family and displays significant selectivity over other bromodomain-containing proteins with notable biochemical activity observed only against BRD9 In cellular assays CPI-637 inhibits MYC expression with an EC50 of 0 60 M and effectively engages CBP in BRET assays (EC50 0 3 M) CPI-637 is currently utilized in preclinical research to investigate the role of CBP/EP300 bromodomains in transcriptional regulation and disease pathways
Cambridge Isotope Laboratories 2 3 4 5 6-PentaBDE (BDE-116) (unlabeled) 50 ug/mL in nonane 1 2 mL
2 3 4 5 6-PentaBDE (BDE-116) (unlabeled) 50 ug/mL in nonane 1 2 mL
eMolecules E-Phenylethenylboronic acid, pinacol ester | Combi-Blocks | 83947-56-2 | MFCD03453666 | 230.110 | C14H19BO2 | 98.000 | CC1(C)OB(OC1(C)C)\C=C\c1ccccc1 | 5g | 117544689
E-Phenylethenylboronic acid, pinacol ester | Combi-Blocks | 83947-56-2 | MFCD03453666 | 230.110 | C14H19BO2 | 98.000 | CC1(C)OB(OC1(C)C)\C=C\c1ccccc1 | 5g | 117544689
![eMolecules Ambeed / transtrans-4-(4-Ethoxy-23-difluorophenyl)-4-ethyl-11-bi(cyclohexane) / 5g / 666598308 / A302043 / / 253199-08-5 / [null] / 350.494 / C22H32F2O](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502424818.PNG-250.jpg)
eMolecules Ambeed / transtrans-4-(4-Ethoxy-23-difluorophenyl)-4-ethyl-11-bi(cyclohexane) / 5g / 666598308 / A302043 / / 253199-08-5 / [null] / 350.494 / C22H32F2O
Ambeed / transtrans-4-(4-Ethoxy-23-difluorophenyl)-4-ethyl-11-bi(cyclohexane) / 5g / 666598308 / A302043 / / 253199-08-5 / [null] / 350.494 / C22H32F2O
Apexbio Technology LLC NMS-873 1418013-75-8 50mg
NMS-873 (CAS 1418013-75-8) is a selective inhibitor of the ATPase VCP/p97 demonstrating inhibitory activity with an IC50 value of 30 nM It targets wild-type VCP as well as VCPC522T mutants without disrupting VCP oligomerization NMS-873 exhibits selectivity against other AAA ATPases HSP90 and various kinases In tumor cell lines including HCT-116 treatment with NMS-873 induces accumulation of polyubiquitinated proteins and stabilization of cyclin E and Mcl-1 leading to altered cell-cycle distribution and reduced cell proliferation NMS-873 shows cytotoxicity across blood cancer and solid tumor cell models (IC50 values 0 08 2 M) supporting its utility in oncology research
![Medchemexpress LLC 1,3,4,5-tetrahydro-4-methyl-6-[1-methyl-3-(1-methyl-pyrazol-4-yl)-indazol-5-yl]-benzodiazepin-2-one | 1884712-47-3 | 100.0% | 386.45 g/mol | C22H22N6O | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000215451.png-250.jpg)
Medchemexpress LLC 1,3,4,5-tetrahydro-4-methyl-6-[1-methyl-3-(1-methyl-pyrazol-4-yl)-indazol-5-yl]-benzodiazepin-2-one | 1884712-47-3 | 100.0% | 386.45 g/mol | C22H22N6O | 1 ML
CPI-637 is a selective, cell-active benzodiazepinone inhibitor of CBP and EP300 bromodomains with potent biochemical activity and demonstrated cellular effects. It inhibits CBP and EP300 with low-nanomolar IC50 values, shows reduced activity against BRD4 BD-1, and is supplied as a concentrated solution for research use.
- Selective CBP and EP300 bromodomain inhibition.
- Potent biochemical activity (low-nanomolar IC50 values).
- Cell-active with measurable EC50 in cellular assays.
- Supplied as a concentrated solution for convenient dosing in assays.
- Suitable for epigenetics and cancer biology research applications.
- Reported high chemical purity for reproducible results.